nac1

NIC3 is a selective nucleus accumbens-associated protein-1 (NAC1) inhibitor with anti-cancer activity.

GLcNAc1-b-PNP is a chromogenic substrate for N-acetyl-β-glucosaminidase and can be used to quantify the activity of N-acetyl-β-D-glucosaminidase in human serum and urine.

MNAC13 is a chimeric mouse IgG1 antibody targeting human TrkA. By specifically binding to the TrkA receptor, MNAC13 inhibits NGF-dependent signaling pathways. It demonstrates effective and lasting analgesic properties, making MNAC13 suitable for research on inflammation and chronic pain.

Fuc1-α-3GlcNAc1-β-Ome is a biochemical reagent used in the study of glycobiology. Glycobiology explores the structure, synthesis, biology, and evolution of sugars. The field encompasses carbohydrate chemistry, glycans' formation and degradation enzymology, protein-glycan recognition, and the role of glycans in biological systems. It is closely connected with fundamental research, biomedical sciences, and biotechnology.

Gal1-β-3GlcNAc1-β-Ome is a type of biochemical reagent used in glycobiology research. Glycobiology explores the structure, synthesis, biology, and evolution of sugars. This field encompasses carbohydrate chemistry, glycan formation and degradation enzymology, protein-glycan recognition, and the role of glycans in biological systems. It closely relates to fundamental research, biomedicine, and biotechnology.

GlcNAc1-β-6GalNAc-α-PNP is a type of biochemical reagent used in glycobiology research. Glycobiology explores the structure, synthesis, biology, and evolution of sugars, encompassing carbohydrate chemistry, glycan formation and degradation enzymology, protein-glycan recognition, and the role of glycans in biological systems. This field is closely associated with fundamental research, biomedicine, and biotechnology.

GalNAc1-b-3Gal-α-Ome (Methyl 3-O-[2-(acetylamino)-2-deoxy-β-D-galactopyranosyl]-α-D-galactopyranoside) is a biochemical reagent utilized in the study of glycobiology. This field explores the structure, synthesis, biology, and evolution of sugars, encompassing carbohydrate chemistry, glycan formation and degradation enzymology, protein-glycan interactions, and the role of glycans in biological systems. Glycobiology is closely linked to fundamental research, biomedical sciences, and biotechnology.

Gal1-β-4GlcNAc1-β-6Gal is a biochemical reagent used in glycoscience research. Glycoscience examines the structure, synthesis, biology, and evolution of sugars. It encompasses carbohydrate chemistry, glycoconjugate formation and degradation enzymology, protein-glycan recognition, and the roles of glycans in biological systems. This field is closely linked to fundamental research, biomedicine, and biotechnology.

GlcNAc1-β-3GalNAc is a reagent used in biochemical reactions.

DNAC-1 is against Gram-positive and Gram-negative pathogens potentiator of β-lactam activity.

GlcNAc 1-P uridyltransferase (CjGlmU), a sugar nucleotidyltransferase (SNT), employs UTP and GlcNAc-1-P to synthesize UDP-GlcNAc, with potential implications in antimicrobial agent research [1].

N-acetylglucosamine-1-P uridyltransferase (AGX1) (GlcNAc1pUT) is a bifunctional enzyme that catalyzes the synthesis of UDP-GlcNAc by coupling GlcNAc-1-P and UTP through an uridyltransfer reaction, exhibiting both acetyltransferase and uridyltransferase activities, and is exclusive to prokaryotes [1].

Diclofenac-13C6 is a 13C6-labeled form of Diclofenac. Diclofenac (T0196) acts as a potent, non-selective anti-inflammatory agent and functions as an inhibitor of COX enzymes. In CHO cells, it has IC50 values of 4 nM for human COX-1 and 1.3 nM for COX-2. Additionally, Diclofenac (T0196) exhibits IC50 values of 5.1 μM for sheep COX-1 and 0.84 μM for COX-2. Dic...

UDP-GlcNAc-13C disodium isodium) is a 13C-labeled version of UDP-GlcNAc disodium (T19596). This compound, also known as UDP-α-D-N-Acetylglucosamine Disodium Salt, serves as a donor substrate for O-GlcNAc transferase (OGT).

GlcNAc 1-P uridyltransferase (PmGlmU) efficiently catalyzes the synthesis of UDP-GlcNAc from GlcNAc-1-P and UTP. In the PmGlmU reaction, it facilitates the breakdown of pyrophosphate into inorganic phosphate to shift the equilibrium of the coupled enzymatic reaction towards the formation of UDP-GlcNAc.